CaTiO3钙钛矿中S/Zr共掺杂促进光催化制氢:光电、热力学和光催化第一性原理研究

IF 1.7 4区 物理与天体物理 Q3 PHYSICS, CONDENSED MATTER
Abdellah Bouzaid, Younes Ziat, Hamza Belkhanchi, Hmad Fatihi
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引用次数: 0

摘要

近年来光催化研究的进展主要集中在开发有效的材料来促进水的分解和氢的产生。本文利用密度泛函理论(DFT)研究了未掺杂和(S, Zr)共掺杂CaTiO3的结构、光电、热力学特性和氧化还原带边缘。初始结构优化结果表明,未掺杂和(S, Zr)共掺杂的CaTiO3具有负的生成能,表明其热力学稳定性。此外,热力学分析表明,共掺杂导致晶格 neisen参数、德拜温度、熵和热容发生了显著变化,表明晶格的非调和性和振动特性随温度和压力的变化而变化。光电计算表明,未掺杂的CaTiO3具有2.77 eV的间接带隙。相比之下,S和Zr共掺杂导致\({{\text{Ca}}_{8}\text{Ti}}_{7}{\text{Zr}}_{1}{\text{O}}_{23}{\text{S}}_{1}\)的直接带隙为2.22 eV, \({{\text{Ca}}_{8}\text{Ti}}_{6}{\text{Zr}}_{2}{\text{O}}_{22}{\text{S}}_{2}\)的直接带隙为1.85 eV,减小了带隙,增强了可见光吸收和光导电性。此外,对Zr-和s -共掺杂CaTiO3的价带和导带边缘位置(EVB和ECB)的分析表明,该材料满足水分解的热力学要求,强调了其作为高效光催化剂的潜力。值得注意的是,随着掺杂剂浓度的增加,观察到的电子和热力学性质的变化呈现出非线性趋势,表明掺杂剂相互作用与主体晶格畸变之间存在复杂的相互作用。这些发现表明,共掺杂材料由于其增强的可见光吸收,在可再生能源应用,特别是太阳能驱动的光催化制氢,光伏器件和光电子学方面表现出很好的性能。图形摘要
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Boosting the photocatalytic hydrogen production via the S/Zr co-doping in a CaTiO3 perovskite: first-principles study of the optoelectronic, thermodynamic, and photocatalytic

Recent advancements in photocatalysis research have mostly concentrated on the development of effective materials to enhance water splitting and the production of hydrogen. This work used density functional theory (DFT) to investigate the structural, optoelectronic, thermodynamic characteristics, and redox band edges of undoped and (S, Zr) co-doped CaTiO3. The initial structural optimization results indicate that undoped and (S, Zr) co-doped CaTiO3 have negative formation energies, signifying their thermodynamic stability. Furthermore, thermodynamic analysis indicates a significant change in the Grüneisen parameter, Debye temperature, entropy, and heat capacities due to co-doping, showing the change of lattice anharmonicity and vibrational characteristics with variations in temperature and pressure. Optoelectronic calculations show that undoped CaTiO3 has an indirect band gap of 2.77 eV. In contrast, co-doping with S and Zr results in direct band gaps of 2.22 eV for \({{\text{Ca}}_{8}\text{Ti}}_{7}{\text{Zr}}_{1}{\text{O}}_{23}{\text{S}}_{1}\) and 1.85 eV for \({{\text{Ca}}_{8}\text{Ti}}_{6}{\text{Zr}}_{2}{\text{O}}_{22}{\text{S}}_{2}\), which reduces the band gap and enhances visible light absorption and optical conductivity. Furthermore, the analysis of the valence and conduction band edge positions (EVB and ECB) of Zr- and S-co-doped CaTiO3 indicates that the material satisfies the thermodynamic requirements for water splitting, underscoring its potential as an efficient photocatalyst. Notably, the observed variations in electronic and thermodynamic properties with increasing dopant concentration reveal a nonlinear trend, suggesting a complex interplay between dopant interactions and host lattice distortions. These findings suggest that co-doped materials exhibit promising properties for renewable energy applications, particularly solar-driven photocatalytic hydrogen production, photovoltaic devices, and optoelectronics, due to their enhanced visible light absorption.

Graphical abstract

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来源期刊
The European Physical Journal B
The European Physical Journal B 物理-物理:凝聚态物理
CiteScore
2.80
自引率
6.20%
发文量
184
审稿时长
5.1 months
期刊介绍: Solid State and Materials; Mesoscopic and Nanoscale Systems; Computational Methods; Statistical and Nonlinear Physics
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